Journal Article
Regulation of ddb2 expression in blind cavefish and zebrafish reveals plasticity in the control of sunlight-induced DNA damage repair
Zhao, H., Li, H., Du, J., Di Mauro, G., Lungu-Mitea, S., Geyer, N., Vallone, D., Bertolucci, C. and Foulkes, N.S.
Record Number:
5207
Year:
2021
Journal:
PLoS Genetics
Volume:
17(2): e1009356
Abstract:
We have gained considerable insight into the mechanisms which recognize and repair DNA
damage, but how they adapt to extreme environmental challenges remains poorly understood.
Cavefish have proven to be fascinating models for exploring the evolution of DNA
repair in the complete absence of UV-induced DNA damage and light. We have previously
revealed that the Somalian cavefish Phreatichthys andruzzii, lacks photoreactivation repair
via the loss of light, UV and ROS-induced photolyase gene transcription mediated by Dbox
enhancer elements. Here, we explore whether other systems repairing UV-induced
DNA damage have been similarly affected in this cavefish model. By performing a comparative
study using P. andruzzii and the surface-dwelling zebrafish, we provide evidence for a
conservation of sunlight-regulated Nucleotide Excision Repair (NER). Specifically, the
expression of the ddb2 gene which encodes a key NER recognition factor is robustly
induced following exposure to light, UV and oxidative stress in both species. As in the case
of the photolyase genes, D-boxes in the ddb2 promoter are sufficient to induce transcription
in zebrafish. Interestingly, despite the loss of D-box-regulated photolyase gene expression
in P. andruzzii, the D-box is required for ddb2 induction by visible light and oxidative stress
in cavefish. However, in the cavefish ddb2 gene this D-box-mediated induction requires
cooperation with an adjacent, highly conserved E2F element. Furthermore, while in zebrafish
UV-induced ddb2 expression results from transcriptional activation accompanied by stabilization
of the ddb2 mRNA, in P. andruzzii UV induces ddb2 expression exclusively via an
increase in mRNA stability. Thus, we reveal plasticity in the transcriptional and post transcriptional
mechanisms regulating the repair of sunlight-induced DNA damage under longterm
environmental challenges.
Times Cited:
2